Package 51655-744-52

Brand: pantoprazole sodium

Generic: pantoprazole
NDC Package

Package Facts

Identity

Package NDC 51655-744-52
Digits Only 5165574452
Product NDC 51655-744
Product ID 51655-744_49515c4d-33ac-58d7-e063-6394a90aa2cc
Description

30 TABLET, DELAYED RELEASE in 1 BOTTLE, PLASTIC (51655-744-52)

Marketing

Marketing Status
Marketed Since 2021-07-09
Brand pantoprazole sodium
Generic pantoprazole
Sample Package No

Linked Drug Pages (1)

PANTOPRAZOLE SODIUM ndc-match (0.95)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "49515c4d-33ac-58d7-e063-6394a90aa2cc", "openfda": {"unii": ["6871619Q5X"], "rxcui": ["251872"], "spl_set_id": ["da67e1c0-9947-957d-e053-2a95a90ad96d"], "manufacturer_name": ["Northwind Health Company, LLC"]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET, DELAYED RELEASE in 1 BOTTLE, PLASTIC (51655-744-52)", "package_ndc": "51655-744-52", "marketing_start_date": "20210709"}], "brand_name": "PANTOPRAZOLE SODIUM", "product_id": "51655-744_49515c4d-33ac-58d7-e063-6394a90aa2cc", "dosage_form": "TABLET, DELAYED RELEASE", "pharm_class": ["Proton Pump Inhibitor [EPC]", "Proton Pump Inhibitors [MoA]"], "product_ndc": "51655-744", "generic_name": "PANTOPRAZOLE", "labeler_name": "Northwind Health Company, LLC", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "PANTOPRAZOLE SODIUM", "active_ingredients": [{"name": "PANTOPRAZOLE SODIUM", "strength": "20 mg/1"}], "application_number": "ANDA202882", "marketing_category": "ANDA", "marketing_start_date": "20210709", "listing_expiration_date": "20271231"}